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2-(2-Bromophenyl)-1,3-Dioxolane

    • Product Name 2-(2-Bromophenyl)-1,3-Dioxolane
    • Alias 2-(2-Bromophenyl)-1,3-dioxolane
    • Einecs 400-110-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    988273

    Chemical Name 2-(2-Bromophenyl)-1,3-dioxolane
    Molecular Formula C9H9BrO2
    Molecular Weight 229.08 g/mol
    Cas Number 52644-14-7
    Appearance Colorless to pale yellow liquid
    Boiling Point 156-158 °C at 15 mmHg
    Density 1.464 g/cm3
    Refractive Index 1.577
    Purity Typically ≥97%
    Solubility Slightly soluble in water, soluble in organic solvents

    As an accredited 2-(2-Bromophenyl)-1,3-Dioxolane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 25g label, white screw cap, hazard symbols, product name “2-(2-Bromophenyl)-1,3-Dioxolane”, supplier details, batch number.
    Shipping 2-(2-Bromophenyl)-1,3-Dioxolane is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported in compliance with chemical safety regulations, typically classified as non-hazardous for air and ground transit, but ensure packaging prevents leaks or breakage during handling. Appropriate labeling and documentation accompany each shipment.
    Storage Store 2-(2-Bromophenyl)-1,3-dioxolane in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizers. Avoid exposure to moisture. Label the container appropriately and keep it away from heat sources and ignition points. Use appropriate protective equipment when handling to prevent skin and eye contact.
    Application of 2-(2-Bromophenyl)-1,3-Dioxolane

    Applications of 2-(2-Bromophenyl)-1,3-Dioxolane in Industrial Manufacturing

    2-(2-Bromophenyl)-1,3-dioxolane serves as a specialty intermediate in several industrial segments, supporting the synthesis of advanced chemical compounds and materials. As the direct manufacturer, we ensure the highest standards of quality and traceability from batch production to global B2B supply. Explore the practical industrial downstream scenarios where this raw material integrates into manufacturing value chains.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Anticonvulsant Synthesis

    Pharmaceutical manufacturers incorporate this dioxolane derivative during the multi-stage synthesis of certain newer-generation anticonvulsant APIs. Its specific structure enables brominated phenyl group introduction, improving molecular selectivity and final product stability through controlled reaction steps. Formulators utilize this material selectively for its reliable behavior during condensation and cyclization, directly impacting isomeric purity and regulatory batch records.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 – FDA cGMP for Finished Pharmaceuticals
    • European Pharmacopoeia (Ph. Eur.) general monographs for API intermediates
    • USP Monographs for related halogenated intermediates, where applicable

    Typical usage ratio

    • 0.3 - 1.5 molar equivalents per API synthesis batch, with final ratio adjusted based on targeted yield and impurity control

    Downstream process integration

    • Material charged during the intermediate condensation step, after initial backbone formation, prior to final cyclization and purification

    Final product types

    • Anticonvulsant tablet and capsule APIs, e.g., brominated phenylpyrrolidones
    • Bulk API intermediates exported for further finishing

    2. Fine Chemical Intermediate for Agrochemical Active Synthesis

    Chemical producers in the agrochemical sector use this aromatic dioxolane to introduce brominated phenyl units within advanced fungicide and insecticide precursor synthesis. The protected dioxolane ring helps control regioselectivity during aromatic substitution, ensuring consistent downstream conversion, while minimizing byproduct formation. Its function in halogen-based activity modulators supports the launch of next-generation crop protection compounds.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical manufacture
    • EC Regulation No 1107/2009 (Plant Protection Products Regulation) for EU market access
    • US EPA Pesticide Registration (40 CFR Part 158) for new active ingredients
    • REACH Regulation, Annex VIII for chemical safety reporting

    Typical usage ratio

    • 5 – 18% mass ratio, typically calculated per key cyclization or halogen exchange cycle

    Downstream process integration

    • Introduced post-initial synthesis as a precursor to key bromination and subsequent dioxolane deprotection steps during active ingredient assembly

    Final product types

    • Fungicide and insecticide chemical actives for grain, fruit, and vegetable protection
    • Bulk pesticide technicals for agrochemical formulation houses

    3. Specialty Monomer Component for Polymeric Materials

    Producers of specialty copolymers and advanced resin blends employ this bromoaromatic dioxolane as a functionalized monomer unit. This material imparts bromine-linked flame retardancy or targeted reactivity to engineered polymer matrices, especially in advanced electronics and automotive materials. The stable cyclic structure allows effective copolymerization, with precise dosing critical to achieve consistent polymer flow and fire classification grades.

    Industry compliance standards

    • UL 94 – Standard for Tests for Flammability of Plastic Materials
    • IEC 60695 (Fire hazard testing for electrical products)
    • RoHS Directive 2011/65/EU on banned substances (excluding regulated brominated compounds)
    • ISO 9001:2015 for polymer manufacturing

    Typical usage ratio

    • 0.5 - 4.7 wt% based on copolymer batch, tunable according to fire resistance class and matrix compatibility

    Downstream process integration

    • Introduced during esterification or copolymerization reaction with acrylics, epoxies, or polyesters under specified heat and agitation profiles

    Final product types

    • Flame retardant resins for electronics encapsulation
    • Automotive interior trim compounds
    • Laminates and coatings with enhanced brominated performance properties

    4. Advanced Material Intermediate for Liquid Crystal Alignment Layers

    Manufacturers of high-precision display components utilize this dioxolane-based intermediate to craft alignment layer formulations for liquid crystal displays (LCDs) and organic electronics. The introduction of a brominated aromatic ring through this precursor enables the formation of anchoring points for surface-treated substrates, improving uniformity and electro-optical consistency in final devices. Process control over molecular orientation and interfacial adhesion relies on precise material dosing at the resin formulation stage.

    Industry compliance standards

    • ISO 9241-307 – Ergonomics of human-system interaction for electronic visual displays
    • IEC 61966 – Electronic display colorimetry
    • ISO 14001 – Environmental management for electronic materials
    • OEM-approved electronic materials protocols

    Typical usage ratio

    • 0.7 - 2.2% wt of total alignment layer solution, optimized after pilot-scale adhesion and LC orientation screening

    Downstream process integration

    • Incorporated at alignment layer resin synthesis stage; post-dispersed into solvent mixes before spin-coating or printing onto display glass panels

    Final product types

    • Liquid crystal display (LCD) alignment coatings
    • Optical-grade surface treated display glass
    • Organic electronics carrier layers
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    Certification & Compliance
    More Introduction

    Understanding 2-(2-Bromophenyl)-1,3-Dioxolane: Manufacturing Perspective and Application Insights

    Decades of Chemical Craft: Why 2-(2-Bromophenyl)-1,3-Dioxolane Stands Out

    From a manufacturer's bench, 2-(2-Bromophenyl)-1,3-dioxolane teaches a direct lesson in the interplay between chemical precision and practical application. Every batch comes from our production lines with a keen awareness of its chemical nuances and broad laboratory appeal. Over the years, certain molecules attract steady interest because they solve real problems—not because of fleeting trends, but for clear, reliable performance in multi-step chemical synthesis, especially in pharmaceutical or agrochemical research. The 1,3-dioxolane group, combined with the 2-bromophenyl ring, forms more than a simple intermediate. This structure brings reactivity and selectivity into sharper focus during many synthesis strategies.

    Our Hands-on Approach: From Raw Inputs to Purity You Can Trust

    Those who mix behind the scenes, scaling from flask to ton scale, know the difference between a sample and a repeatable process. Raw phenyl derivatives often carry trace contaminants. Even slight bromination inconsistencies can change downstream behavior. In our facility, quality controls span the journey—each fraction checked for byproducts that might trip up a demanding reaction step. The dioxolane ring forms through controlled acetalization, protecting the aldehyde group of the parent compound. This step not only boosts stability during complex syntheses, but it also translates to better yields for end users testing route development or scaling pilot runs.

    Why This Molecule Draws Persistent Industry Attention

    Few molecules fill a niche on purpose and by necessity. Over our years working with academic, biotech, and industrial chemists, 2-(2-Bromophenyl)-1,3-dioxolane has proven a recurrent favorite in multi-step synthesis where protection, selectivity, and substitution matter. A core reason: the bromo group, sitting ortho to the dioxolane, directs subsequent reactions in cross-coupling or functional group exchange. Researchers tell us time and again—when they need to safeguard sensitive aldehydes and still hold onto a reactive handle, this compound features on their bench.

    Its main competition? Simple brominated benzenes or dioxolane-protected aldehydes lacking the ortho-bromo group. From daily experience, we observe shortcomings with those alternatives. Without the dual protection and reactivity that this molecule offers, chemists often fight side reactions, lower selectivity, or stepwise protection–deprotection headaches. Instead, this hybrid lets our partners streamline synthetic schemes, minimize purification chores, and keep cost per gram in check when scaling.

    Pushing Purity Boundaries: Setting Our Own Standards

    Picture the load that crosses our analytical instruments: NMR, HPLC, GC checks run for every batch. Even trace levels of unreacted starting material—sometimes measured in tenths of a percent—show up in sensitive reactions downstream. The pressure dioxolane ring has another job: it doesn’t just act as a passive bystander. In many syntheses, the acetal ring survives robust base or acid treatments, letting users carry the protection through long routes. We keep residual impurity targets extremely tight in our spec sheets, not out of obligation, but because we see how customers’ yields and reproducibility take a hit otherwise.

    Years of feedback say more than any label claim. Gram-scale labs or pilot plants aren’t keen on surprises halfway through a pivotal scale-up. In today’s tightly regulated laboratory landscape, that reliability forms a hidden strength far outlasting the stack of COAs. If trace impurities slip through, it’s not just an internal concern; in some cases, it ruins days or weeks of effort for a customer.

    How Reactivity Profile Defines Real-World Value

    On paper, many intermediates look interchangeable, at least to those used to reading catalogs. Reality in synthesis often runs rougher. Take direct arylation, for instance: the ortho-bromo on our dioxolane opens a shortcut for Suzuki or Buchwald-Hartwig cross-couplings. Chemists can introduce new aryl or amine couplings there, all while the dioxolane quietly shields sensitive groups. Many customers describe the simple time savings as “weeks in a bottle.” Instead of juggling multiple protection and deprotection strategies, the molecule supports step economy, a trend research labs and production plants want as margins tighten.

    Contrast that with non-dioxolane-protected bromobenzenes. Once subjected to strong bases or acids, those often succumb to unwanted side reactions, especially hydrolysis or polymerization under less-than-dry conditions. With our product, those headaches drop off—yield and selectivity stay robust, even when conditions drift slightly off ideal, as happens in almost every real manufacturing environment.

    Where the Chemistry Meets Regulatory and Operational Reality

    Many forget a production chemist’s concerns extend well past synthetic yield. Trace moisture, air exposure, hazardous solvents—all pose risks that can cause unwanted transformations during storage or shipping. We see the dioxolane ring as more than functional decoration. It provides real-world stability, extending shelf life, avoiding decomposition, and reducing hazardous byproducts. Rather than shipping expensive material that risks spoilage or regulatory headaches, we focus on protected intermediates like this, because customers downstream expect reliability months after delivery.

    Even packaging counts here. Bulk shipments use lined steel or polypropylene drums, chosen to guard against contamination and prevent interactions that would eat into quality. Smaller lab-scale bottles arrive in certified glass with air-tight seals, always purged with inert gas. We’ve learned over years that one leaky stopper can wipe out the shelf life of a precious intermediate; packing teams treat every request like a time-sensitive asset, not a warehouse formality.

    A Look Inside: Crafting, Verifying, and Scaling the Process

    In our own workflows, the day doesn’t end after a single synthesis or scale-up. Teams work through multiple synthetic routes—not every condition optimizes well at both pilot and production scales. Some routes favor gentle, catalytic bromination with ultra-clean starting materials, others respond better to batch processing under closely monitored reflux. Every method gets scored for conversion yield, impurity profile, product isolation, and downstream compatibility.

    We understand today’s customers have strict process validation needs. Analytical chemists in our labs spend hours tracking the composition at every stage: monitoring NMR integrations, running IR for functional group confirmation, and cross-checking with GC to catch trace volatiles. Each time we discover a new side product, tweaks follow. This iterative process repeats batch after batch—not just with an eye for improving yields, but to catch the edge cases where a customer’s process interacts with a rare impurity.

    Specification Isn’t Just a List: It's Lessons Remembered

    Real confidence in a batch doesn’t come from a line on a checklist. Experience says it grows with every shipment that arrives exactly as expected, backed by an honest log of tests and observations. We work closely with customers and partners to build practical specifications—clarity about melting points, limits on related substances, and defining exactly what “acceptable off-white solid” means in practice.

    Sometimes, we receive requests asking for even stricter impurity control or alternate crystalline forms. Our team goes back to the drawing board, trialing alternate recrystallizations, switching solvents, adjusting drying conditions, and extending shelf-life tests. Feedback doesn’t sit in a folder; it guides the process forward so the next batch improves, step by step. Specs emerge from actual problems solved, not from wishful thinking or marketing gloss.

    Handling and Storage: Details Built on Years of Practice

    Every gram that leaves our site benefits from experience handling moisture-sensitive and halogenated organics. Warehouse staff catalog materials in controlled environments, keeping humidity and temperature within strict ranges. We’ve seen what happens when these controls slip—clumping, discoloration, or in some cases, product degradation. Shipments head out accompanied by desiccant packs, thermal protection in summer and winter, and documentation on proper storage.

    Customers handling developmental quantities often run pilot projects, and regular feedback loops mean storage suggestions adjust alongside real-world needs. Some users run at open bench scale and may request custom vialing or smaller aliquots. Others need bulk units fit for kilo-scale reactors, packaged in a way that lets automated feeders dispense material without bridging or sticking. We document stability profiles under a range of conditions so users in diverse geographies can rely on the same product performance.

    Supporting Customers: More Than a Transaction

    Too many suppliers focus on the sale, not on how a molecule fits into the tough, sweaty routines of research or production. As a manufacturer, we know both sides of the fence: stubborn reaction byproducts, inconsistent yields, and the agony of failing at scale. Direct customer calls often surface root causes that don’t appear in glowing literature—trace water in a drum or a misleading spectral blip that derails advanced characterization.

    Technical support draws on the full archive of our production notes. If a formulator finds an unexpected impurity, our lab can track back to batch numbers, synthesis logs, and storage conditions, offering insight that speeds troubleshooting. We keep communication clear and honest—never hiding behind jargon or brush-off explanations. Our intention is simple: to make trials smoother and routine production runs less uncertain.

    When scale-up challenges appear, sometimes it’s not just the chemistry but the logistics—custom packaging, transport at specific temperatures, or coordinating multi-lot releases to keep a continuous supply line. We commit resources to resolve these, knowing the cost of downtime or batch-to-batch inconsistency can ripple throughout a project. For certain applications, we offer documentation or testing beyond standard certification: limited residual solvent or bioburden testing, stability data under field-specific conditions, and transport validation for regulatory compliance.

    Looking Beyond: Environmental and Safety Mindset in Manufacturing

    Our teams think hard about the entire product lifecycle, not just the chemistry. Waste management, effluent treatment, safe handling of halogenated by-products—each part of our process minimizes risk to operators and the environment. We’ve invested in closed-system transfer for brominated intermediates, in-house scrubbers for emissions, and safe solvent recovery processes that reduce hazardous waste and energy consumption. In an industry facing resource constraints and stricter regulations every year, environmental responsibility isn’t just compliance, it’s survival.

    We get requests for greener synthesis routes or alternate solvent systems. These aren’t always simple to provide—halogenated aromatics have real toxicity and waste handling challenges. Our process improvement teams keep searching for catalysts and conditions that favor less waste and better atom economy, with a steady eye on worker safety and emissions. Customer curiosity sometimes sparks new initiatives—requests for non-halogenated analogs or lower residual solvent content prompt us to explore out-of-the-box solutions, even if the commercial path takes time.

    R&D Partnerships: The Engine for Next-Generation Molecules

    Science moves because people collaborate directly. Our R&D team partners with synthetic chemists working on everything from API candidates to crop protection scaffolds. They share both victories and setbacks using our products. The feedback loop here shortens the story from “problem observed” to “solution built in.” Some users hit bottlenecks in coupling efficiency, find unexpected interactions with catalysts, or want to test unconventional reaction partners. Our technical team often steps in to devise new synthetic approaches or customize product attributes so users solve these bottlenecks faster.

    Sometimes, this means tweaking the bromo/dioxolane ratio, adjusting crystal forms, or testing alternative protection groups with compatible reactivity. Not every request produces a commercial product, but the cumulative learning keeps us ahead of shifts in industrial need. Access to pilot facilities speeds scale-up of promising variations, with honest feedback returned to both ends of the supply chain. Direct, transparent engagement with innovators at the bench pushes us to deliver molecules that don’t just fit a spec sheet—they make someone’s synthesis faster, cheaper, and more resilient.

    Cutting Through the Noise: How Our Experience Translates to Value

    The difference isn’t just a price tag or purity number. It’s the sum of tough lessons learned scaling chemistry from a 100-gram flask to 100-liter reactors. It’s recognizing that even a “minor” impurity—barely visible in a spectrum—can cause a separation headache in a downstream column or a regulatory letter years later. It’s responding when a formulation team on another continent needs assurance that this batch of 2-(2-Bromophenyl)-1,3-dioxolane behaves just like the one they tested months ago.

    With laboratories around the world demanding shorter timelines, smaller footprints, and fewer supply chain hiccups, the chemistry behind each batch becomes personal. We see it as more than molecules moving along a conveyor. Every drum shipped, every sample dispatched, carries the trust and expectation of a user whose project depends on our attention to making things right. Years in the market build perspective: no shortcut replaces discipline, consistency, and constant learning.

    Continuous Improvement: The Only Way Forward

    Making chemical intermediates that actually help people do creative transformational chemistry is not a set-it-and-forget-it business. Customer needs evolve as new green chemistry mandates emerge, as downstream targets get more complex, and as regulatory scrutiny digs deeper. We keep a living history of improvement projects—sometimes shifting a single raw material source, other times completely overhauling a purification step because a customer found a better way.

    Our own teams value ongoing education and training; many technicians have spent years honing their skills in dioxolane chemistry, bromination, crystallization, and analytical development. This dedication translates to products designed to handle real-world variables, not just lab-bench precision. As new uses for brominated dioxolane derivatives emerge—ranging from advanced catalyst development to specialty material synthesis—we keep our ears open and our processes ready to adapt.

    Distinctiveness in a Crowded Marketplace

    Those working with 2-(2-Bromophenyl)-1,3-dioxolane recognize quickly that not all suppliers value control throughout the chain of manufacturing. Trader and catalog resellers sometimes repackage materials acquired from multiple levels away, leading to inconsistencies and hard-to-trace quality complaints. By contrast, handling every stage from raw procurement to finished goods gives us direct accountability. Since every customer outcome reflects directly on our team, we keep processes transparent and open to scrutiny.

    User feedback frames the most common complaints with commodity alternatives: batch variance, inconsistent melting points, high-level contamination, and unreliable lead times. In response, our approach keeps everything in-house as far as reasonable, supported by validated contract testing for specialized requirements. It’s not just pride of authorship—it’s a route to fewer mistakes and better long-term relationships with the laboratories and production lines relying on this versatile molecule.

    Final Thoughts from the Factory Floor

    Experience proves that in chemical manufacturing, the intersection of technical performance, process discipline, and direct feedback separates routine intermediates from trusted tools. 2-(2-Bromophenyl)-1,3-dioxolane earns returning customers not because of promises, but because its chemical behavior, reliability, and results in synthetic sequences speak for themselves.

    We see our role extending beyond producing grams or kilos; it’s about reducing experimentation risk, smoothing the path for pilot and production scale-ups, and enabling new chemistry with consistent, thoughtfully crafted intermediates. As labs and factories across the world look for ways to move faster and more sustainably, every step taken to tighten process control, innovate reactively, and learn from each user’s journey pays off in better chemistry—and stronger results—for everyone involved.